Canonical Allele Identifier: CA341278278
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-94001932-T-G
MyVariant Identifiers: chr1:g.94467488T>G (hg19) chr1:g.94001932T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94001932T>G , CM000663.2:g.94001932T>G GRCh38
NC_000001.10:g.94467488T>G , CM000663.1:g.94467488T>G GRCh37
NC_000001.9:g.94240076T>G NCBI36
NG_009073.1:g.124218A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6208A>C MANE Select ENSP00000359245.3:p.Thr2070Pro
ENST00000370225.3:c.6208A>C ENSP00000359245.3:p.Thr2070Pro
ENST00000465352.1:n.624A>C
ENST00000536513.5:c.2584A>C ENSP00000439707.2:p.Thr862Pro
NM_000350.2:c.6208A>C NP_000341.2:p.Thr2070Pro
NM_000350.3:c.6208A>C MANE Select NP_000341.2:p.Thr2070Pro
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